Canonical Allele Identifier: CA406655731
Community Standard Title: NM_001364171.2(ODAD1):c.1426G>T (p.Ala476Ser)
Gene: ODAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48298076C>A , CM000681.2:g.48298076C>A GRCh38
NC_000019.9:g.48801333C>A , CM000681.1:g.48801333C>A GRCh37
NC_000019.8:g.53493145C>A NCBI36
NG_033251.1:g.27000G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001364171.2:c.1426G>T MANE Select NP_001351100.1:p.Ala476Ser
ENST00000674294.1:c.1426G>T MANE Select ENSP00000501363.1:p.Ala476Ser
NM_001364171.1:c.1426G>T NP_001351100.1:p.Ala476Ser
NM_144577.3:c.1315G>T NP_653178.3:p.Ala439Ser
NM_144577.4:c.1315G>T NP_653178.3:p.Ala439Ser
ENST00000315396.7:c.1315G>T ENSP00000318429.7:p.Ala439Ser
ENST00000474199.5:n.1443G>T
ENST00000474199.6:c.1426G>T ENSP00000501357.1:p.Ala476Ser
ENST00000497273.1:n.842G>T
ENST00000674207.1:c.*1112+101G>T ENSP00000501374.1:n.*1112+101G>T
XM_005259413.2:c.1426G>T XP_005259470.1:p.Ala476Ser
XM_005259414.2:c.1426G>T XP_005259471.1:p.Ala476Ser
XM_005259414.3:c.1426G>T XP_005259471.1:p.Ala476Ser
XM_005259415.2:c.1426G>T XP_005259472.1:p.Ala476Ser
XM_005259415.3:c.1426G>T XP_005259472.1:p.Ala476Ser
XM_005259416.3:c.742G>T XP_005259473.1:p.Ala248Ser
XM_005259416.4:c.742G>T XP_005259473.1:p.Ala248Ser
XM_011527515.1:c.1315G>T XP_011525817.1:p.Ala439Ser
XM_011527515.2:c.1315G>T XP_011525817.1:p.Ala439Ser
XM_011527516.1:c.1315G>T XP_011525818.1:p.Ala439Ser
XM_011527516.2:c.1315G>T XP_011525818.1:p.Ala439Ser
XM_017027483.1:c.1150G>T XP_016882972.1:p.Ala384Ser
XM_024451782.1:c.1465G>T XP_024307550.1:p.Ala489Ser
XM_024451783.1:c.1426G>T XP_024307551.1:p.Ala476Ser